Human factors research and design service that optimizes medical device usability and user interface through systematic analysis, testing, and design methodology. Supports regulatory compliance with international standards for human factors validation in medical product development.
Manufactured by
Emergo by UL
Austin TX, United States
Emergo by UL offers a single-source solution for bringing medical devices to established and emerging markets. Choose from either SaaS or traditional consulting options to help manage your business. Your partner for medical device, in-vitro diagnostic regulatory affairs management Emergo was founded in 1997 with a mission to help medical device and IVD manufacturers manage regulatory affairs compliance and expand into new markets. We have grown into a global solutions provider specializing in end-to-end regulatory affairs/quality assurance life cycle management. Our unique services include local project managers and local sales teams partnering with global RA/QA experts for product lifecycle management. In 2017, UL Solutions acquired Emergo. UL Solutions depth and breadth of nonclinical testing expertise complements Emergo s global device registration, quality management, in-country representation, and related services. By joining the UL enterprise, Emergo can offer customers more comprehensive support for medical device registration, QMS compliance and now, nonclinical testing and certification to get products to market faster.
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WILDDESIGN GmbH
Germany · 2 relevant products
OSMUNDA Medical Device Service Group
China · 1 relevant product
TS Quality & Engineering SRL
Italy · 3 relevant products
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3 of 90 closest product alternatives
WILDDESIGN GmbH · Germany
Medical device design and development services specializing in product design, UX design, and usability engineering for medical technology. Supports the full design lifecycle from concept through regulatory compliance and market launch.
OSMUNDA Medical Device Service Group · China
Research and design service for medical device development, offering end-to-end innovation solutions from concept through prototype and commercialization. Supports regulatory compliance, feasibility assessment, and product optimization for healthcare technology development.
TS Quality & Engineering SRL · Italy
Comprehensive medical device consulting services covering design control, risk management, regulatory compliance (MDR, MDSAP), quality management systems (ISO 13485), and market introduction support. Services include mechanical design, FEA analysis, prototyping, DHF documentation, UDI implementation, and EUDAMED registration to facilitate product development from concept through global commercialization.
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